Iron (Fe) minerals are known to be effective adsorbents for arsenic (As). However, the effects of sulfur species formed from the reductive dissolution of Fe minerals on the transformation of As(III) during the redox fluctuations processes under ambient conditions were poorly understood. Herein, we synthesized the As(III)-Fe minerals using sodium arsenite and ferric nitrate to investigate the effects of sulfur species on As(III) transformation in the As(III)-Fe minerals. Experimental results showed that sulfite rather than elemental sulfur and thiosulfate significantly accelerated As(III) oxidation. The oxidation rate of As(III) increased markedly from 0.0050 to 0.0168 min with the increase of sulfite concentration from 0.5 to 2.0 mM. Sulfate radicals (SO) and hydroxyl radicals (OH) were identified as the dominant reactive species for As(III) oxidation. Besides, the underlying mechanism of Fe(II)/Fe(III) cycling for enhancing As(III) oxidation was further explored in the homogeneous Fe(II)/sulfite systems. Finally, interactions between sulfite and soil components induced radical formation, leading to As(III) oxidation in the soil environments. This study gives new insights into As(III) transformation co-existed with Fe minerals and sulfur species, which shed light on developing remediation strategies for regulating As contamination in temporarily flooded soils. ENVIRONMENTAL IMPLICATION: "New Insights into the Mechanism of Sulfur Species Induced As(III) Oxidation in the As-Fe Minerals" This study systematically explored the coupled effects between sulfur species and Fe minerals on As(III) transformation in the As-Fe-minerals under oxic conditions, which showed that sulfite significantly accelerated As(III) oxidation to As(V) via the enhanced formation reactive oxygen species (e.g., SO and OH). This study shed light on the development of remediation strategies in the contaminated soils with toxic pollutants via introducing sulfur species. We strongly believe this study is of great interest to environmental scientists and chemical engineers, especially those who works on the remediation of contaminated sites and wish to explore the high-efficiency strategies for the control of toxic pollutants like As.
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http://dx.doi.org/10.1016/j.jhazmat.2023.133292 | DOI Listing |
J Environ Sci (China)
August 2025
School of Energy and Environmental Engineering, University of Science and Technology Beijing, Beijing 100083, China; Beijing Key Laboratory of Resource-oriented Treatment of Industrial Pollutants, University of Science and Technology Beijing, Beijing 100083, China.
Arsenic and cadmium contamination frequently coexist in the real environment. However, it remains a challenge for their simultaneous removal due to their distinct physicochemical properties at low cost. To this end, a cost-effective magnetic biochar adsorbent (ITBNa800) was prepared using biomass waste and iron tailings slag.
View Article and Find Full Text PDFEnviron Pollut
March 2025
Division of Sustainable Resources Engineering, Faculty of Engineering, Hokkaido University, Sapporo, 060-8628, Japan.
An effective and ingenious method called "snow-melting" system was widely implemented for snow management in the Ishikari Plain, Japan. In this system, groundwater is pumped up, mixed with snow, and discharged into a nearby river. Since the groundwater in the Ishikari Plain is contaminated with arsenic (As), the impacts of directly discharging As-bearing groundwater into the river were assessed and monitored.
View Article and Find Full Text PDFEnviron Sci Technol
March 2025
Geomicrobiology, Department of Geosciences, University of Tuebingen, Tuebingen 72076, Germany.
The reduction of As(V) to As(III) has been proposed as an undesirable process, increasing the mobility and toxicity of arsenic. Although most studies revealed that As(V) reduction occurs in the aqueous phase, it remains unclear whether abiotic As(V) reduction driven by minerals in drought environments also exists. In this study, we examined the transformation of As(V) to As(III) mediated by ferrihydrite during drying processes using high-resolution X-ray photoelectron spectroscopy (XPS) and X-ray absorption near edge structure (XANES) spectroscopy analyses.
View Article and Find Full Text PDFJ Hazard Mater
February 2025
Department of Environment and Energy and Soil Environment Research Center, Jeonbuk National University, 567 Baekje-daero, Deokjin, Jeonju, Jeollabukdo 54896, Republic of Korea. Electronic address:
In-situ electrochemical remediation has emerged as a promising groundwater remediation technology. However, its application has been limited to short-term decontamination. Here, we propose an electrochemical system that combines an e-barrier with pyrite, a sulfide mineral capable of completely removing As(III), Cr(VI), and sulfanilamide continuously for one year.
View Article and Find Full Text PDFJ Hazard Mater
February 2025
Key Laboratory of Environmental Pollution Monitoring and Disease Control, Ministry of Education, School of Public Health, Guizhou Medical University, Guiyang 561113, China; Collaborative Innovation Center for Prevention and Control of Endemic and Ethnic Regional Diseases Co-constructed by the Province and Ministry, Guizhou Medical University, Guiyang 561113, China. Electronic address:
Arsenic (As) and heavy metal contamination in aquatic systems pose critical environmental challenges, particularly in reservoirs. This study utilized dual-sided high-resolution diffusive gradients in thin films (DGT) probes on-site to investigate the spatial distribution and mobility of As species and heavy metals (Cd, Cr, Cu, Ni, Pb, Sb, and Zn) in the Hongfeng Reservoir, a deep karst reservoir in southwest China. Results revealed that As mobility was primarily governed by redox-sensitive processes, including the reduction of As(V) to As(III) and the reductive dissolution of Fe/Mn oxides.
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